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FDA settles drug compounding suit, agrees to speed its review of bulk ingredients

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FDA settles drug compounding suit, agrees to speed its review of bulk ingredients

Back in 2014, the FDA made very clear to the growing but under-regulated pharma compounding world that it would begin implementing a new law from Congress requiring the agency to develop a list of bulk drug substances (or active ingredients) that companies may use to compound drugs. But the nomination

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review critic pharma drugs medecine pharmaceutical fda public health public safety united states usa compounding bulk ingredients

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FDA settles drug compounding suit, agrees to speed its review of bulk ingredients

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FDA settles drug compounding suit, agrees to speed its review of bulk ingredients

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